FDAFDA · Food and drugs·Recall number D-0078-2018
Lumigan (bimatoprost ophthalmic solution) 0.01%, 2.5 mL bottle, Rx only, Allergan, Irvine, CA 92612. NDC# 0023-3205-03
Published November 22, 2017 · Recall initiated: October 19, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LUMIGAN
- Manufacturer
- Allergan Sales, LLC
- Distributor
- Nationwide and Barbados, Curacao, Dominican Republic, Guyana, Jamaica, and Trinidad and Tobago.
- Lot
- Lot #: 92575 Exp. JUN-2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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